Have questions? Visit https://www.reddit.com/r/SNPedia

rs863223811

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223811(C;C)
Make rs863223811(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position99137980
GeneTGFBR1
is asnp
is mentioned by
dbSNPrs863223811
ebirs863223811
HLIrs863223811
Exacrs863223811
Varsomers863223811
Maprs863223811
PheGenIrs863223811
hapmaprs863223811
1000 genomesrs863223811
hgdprs863223811
ensemblrs863223811
gopubmedrs863223811
geneviewrs863223811
scholarrs863223811
googlers863223811
pharmgkbrs863223811
gwascentralrs863223811
openSNPrs863223811
23andMers863223811
23andMe allrs863223811
SNP Nexus

SNPshotrs863223811
SNPdbers863223811
MSV3drs863223811
GWAS Ctlgrs863223811
Max Magnitude0
ClinVar
Risk rs863223811(C;C)
Alt rs863223811(C;C)
Reference rs863223811(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.101900262G>C
CLNSRC
CLNACC RCV000200533.1,